| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs60261494 | 0.882 | 0.080 | 8 | 24956493 | missense variant | GG/CT | mnv | 2 | |||
| rs11575937 | 0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv | 1 | |||
| rs145770066 | 0.882 | 0.080 | 19 | 49830790 | missense variant | C/T | snv | 3.8E-03 | 4.3E-03 | 1 |